Leucine improves protein nutritional status and regulates hepatic lipid metabolism in calorie-restricted rats

Cell Biochem Funct. 2014 Jun;32(4):326-32. doi: 10.1002/cbf.3017. Epub 2013 Dec 11.

Abstract

Several studies have highlighted the potential of leucine supplementation for the treatment of metabolic diseases including type 2 diabetes and obesity. Caloric restriction is a common approach to improve the health in diabetic and obese subjects. However, very few studies assessed the effects of leucine supplementation in calorie-restricted animals. Rats were subjected to a 30% calorie-restricted diet for 6 weeks to study the effects of leucine supplementation on protein status markers and lipid metabolism. Caloric restriction reduced the body weight. However, increased leucine intake preserved body lean mass and protein mass and improved protein anabolism as indicated by the increased circulating levels of albumin and insulin-like growth factor-1 (IGF-1), and the liver expression of albumin and IGF-1 messenger RNA. Leucine supplementation also increased the circulating levels of interleukin-6 and leptin but did not affect the tumour necrosis factor-α and monocyte chemotactic protein-1 concentrations. Ketone bodies were increased in rats consuming a leucine-rich diet, but we observed no changes in cholesterol or triglycerides concentrations. Caloric restriction reduced the liver expression of peroxisome proliferator activated receptor-α and glucose-6-phosphatase, whereas leucine supplementation increased the liver expression of 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMG-CoA) reductase and sterol regulatory element-binding transcription factor 1. A leucine-rich diet during caloric restriction preserved whole body protein mass and improved markers of protein anabolism. In addition, leucine modulated the hepatic lipid metabolism. These results indicate that increased leucine intake may be useful in preventing excessive protein waste in conditions of large weight loss.

Keywords: IGF-1; albumin; branched-chain amino acids; caloric restriction; interleukin-6; supplementation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumins / genetics
  • Albumins / metabolism
  • Animals
  • Biomarkers / metabolism
  • Body Composition
  • Caloric Restriction
  • Dietary Supplements*
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Interleukin-6 / blood
  • Ketone Bodies / metabolism
  • Leptin / blood
  • Leucine / pharmacology*
  • Lipid Metabolism*
  • Liver / metabolism*
  • Male
  • Nutritional Status*
  • RNA, Messenger / metabolism
  • Rats, Sprague-Dawley
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Albumins
  • Biomarkers
  • Interleukin-6
  • Ketone Bodies
  • Leptin
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Insulin-Like Growth Factor I
  • Leucine